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Tirzepatide for Obesity Treatment and Diabetes Prevention.

Jastreboff AM, et al. · 2025
PubMed 39536238 ↗DOI: 10.1056/NEJMoa2410819The New England journal of medicine
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💊 Lavora su: Terapia · lente Traiettoria · il corpo nel tempo
tocca anche ⚖️ Peso & grasso viscerale
RCT (prova forte)
La domanda

In persone con obesita e prediabete, il trattamento prolungato con tirzepatide riduce il peso e rallenta la progressione a diabete di tipo 2 rispetto al placebo?

Cosa hanno trovato

RCT di fase 3 in doppio cieco (SURMOUNT-1), n=2539 con obesita, di cui 1032 anche con prediabete (oggetto di questa analisi), randomizzati 1:1:1:1 a tre dosaggi di tirzepatide o placebo, per 176 settimane piu 17 settimane off-treatment. A 176 settimane il calo ponderale medio con tirzepatide va da -12,3% a -19,7% (dosi crescenti) vs -1,3% con placebo (P<0,001 per tutti i confronti). Diagnosi di T2D: 1,3% con tirzepatide vs 13,3% placebo, HR 0,07 (IC 95% 0,0-0,1; P<0,001). Dopo 17 settimane dalla sospensione: 2,4% vs 13,7%, HR 0,12 (IC 95% 0,1-0,2; P<0,001). Eventi avversi piu comuni gastrointestinali, per lo piu lievi-moderati e concentrati nella fase di titolazione; nessun nuovo segnale di sicurezza.

Cosa significa per te

Vale per la prevenzione del tipo 2 in chi ha obesita e prediabete. Il farmaco produce calo di peso marcato e riduce fortemente il passaggio a T2D; dopo la sospensione una parte del rischio riemerge (2,4% vs 13,7%), segno che il beneficio e legato al trattamento in corso. Onesta sulla prova: RCT di fase 3 (prova forte), ma questa e l'analisi del sottogruppo obesita+prediabete di uno studio finanziato dal produttore. Trattandosi di un farmaco, indicazione, avvio e sospensione sono decisione del diabetologo.

Abstract (in lingua originale)

BACKGROUND: Obesity is a chronic disease and causal precursor to myriad other conditions, including type 2 diabetes. In an earlier analysis of the SURMOUNT-1 trial, tirzepatide was shown to provide substantial and sustained reductions in body weight in persons with obesity over a 72-week period. Here, we report the 3-year safety outcomes with tirzepatide and its efficacy in reducing weight and delaying progression to type 2 diabetes in persons with both obesity and prediabetes. METHODS: We performed a phase 3, double-blind, randomized, controlled trial in which 2539 participants with obesity, of whom 1032 also had prediabetes, were assigned in a 1:1:1:1 ratio to receive tirzepatide at a once-weekly dose of 5 mg, 10 mg, or 15 mg or placebo. The current analysis involved the participants with both obesity and prediabetes, who received their assigned dose of tirzepatide or placebo for a total of 176 weeks, followed by a 17-week off-treatment period. The three key secondary end points, which were controlled for type I error, were the percent change in body weight from baseline to week 176 and onset of type 2 diabetes during the 176-week and 193-week periods. RESULTS: At 176 weeks, the mean percent change in body weight among the participants who received tirzepatide was -12.3% with the 5-mg dose, -18.7% with the 10-mg dose, and -19.7% with the 15-mg dose, as compared with -1.3% among those who received placebo (P<0.001 for all comparisons with placebo). Fewer participants received a diagnosis of type 2 diabetes in the tirzepatide groups than in the placebo group (1.3% vs. 13.3%; hazard ratio, 0.07; 95% confidence interval [CI], 0.0 to 0.1; P<0.001). After 17 weeks off treatment or placebo, 2.4% of the participants who received tirzepatide and 13.7% of those who received placebo had type 2 diabetes (hazard ratio, 0.12; 95% CI, 0.1 to 0.2; P<0.001). Other than coronavirus disease 2019, the most common adverse events were gastrointestinal, most of which were mild to moderate in severity and occurred primarily during the dose-escalation period in the first 20 weeks of the trial. No new safety signals were identified. CONCLUSIONS: Three years of treatment with tirzepatide in persons with obesity and prediabetes resulted in substantial and sustained weight reduction and a markedly lower risk of progression to type 2 diabetes than that with placebo. (Funded by Eli Lilly; SURMOUNT-1 ClinicalTrials.gov number, NCT04184622.).
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